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Journal Abstract Search

266 related items for PubMed ID: 30577453

  • 1. Adaptive Immunodeficiency in WHIM Syndrome.
    Majumdar S, Murphy PM.
    Int J Mol Sci; 2018 Dec 20; 20(1):. PubMed ID: 30577453
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  • 2. CXCL12/CXCR4-axis dysfunctions: Markers of the rare immunodeficiency disorder WHIM syndrome.
    Bachelerie F.
    Dis Markers; 2010 Dec 20; 29(3-4):189-98. PubMed ID: 21178277
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  • 6. WHIM syndrome: congenital immune deficiency disease.
    Kawai T, Malech HL.
    Curr Opin Hematol; 2009 Jan 20; 16(1):20-6. PubMed ID: 19057201
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  • 7. The CXCR4 mutations in WHIM syndrome impair the stability of the T-cell immunologic synapse.
    Kallikourdis M, Trovato AE, Anselmi F, Sarukhan A, Roselli G, Tassone L, Badolato R, Viola A.
    Blood; 2013 Aug 01; 122(5):666-73. PubMed ID: 23794067
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  • 8. Genetics on a WHIM.
    Al Ustwani O, Kurzrock R, Wetzler M.
    Br J Haematol; 2014 Jan 01; 164(1):15-23. PubMed ID: 24111611
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  • 9. Altered leukocyte response to CXCL12 in patients with warts hypogammaglobulinemia, infections, myelokathexis (WHIM) syndrome.
    Gulino AV, Moratto D, Sozzani S, Cavadini P, Otero K, Tassone L, Imberti L, Pirovano S, Notarangelo LD, Soresina R, Mazzolari E, Nelson DL, Notarangelo LD, Badolato R.
    Blood; 2004 Jul 15; 104(2):444-52. PubMed ID: 15026312
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  • 15. G protein-coupled receptor kinase-3-deficient mice exhibit WHIM syndrome features and attenuated inflammatory responses.
    Tarrant TK, Billard MJ, Timoshchenko RG, McGinnis MW, Serafin DS, Foreman O, Esserman DA, Chao NJ, Lento WE, Lee DM, Patel D, Siderovski DP.
    J Leukoc Biol; 2013 Dec 15; 94(6):1243-51. PubMed ID: 23935208
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